Αποτελέσματα αναζήτησης - "ПЕРИОДИЧЕСКАЯ ЛИХОРАДКА"

1

Academic Journal

РFАРА–syndrome: a literature review and own clinical observation

Συγγραφείς: D.S. Khapchenkova, S.О. Dubyna

Πηγή: Сучасна педіатрія. Україна; № 6(110) (2020): Сучасна педіатрія. Україна; 57-61
Modern Pediatrics. Ukraine; № 6(110) (2020): Modern pediatrics. Ukraine; 57-61
Современная педиатрия. Украина; № 6(110) (2020): Современная педиатрия. Украина; 57-61

Θεματικοί όροι: Marshall's syndrome, children, periodic fever, corticosteroids, синдром Маршалла, дети, периодическая лихорадка, глюкокортикоиды, діти, періодична лихоманка, глюкокортикоїди, 16. Peace & justice, 3. Good health

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Σύνδεσμος πρόσβασης: https://med-expert.com.ua/journals/wp-content/uploads/2020/12/10-1.pdf
http://mpu.med-expert.com.ua/article/view/SP.2020.110.57

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2

Academic Journal

PFAPA-синдром (синдром Маршалла) у ребенка 1,6 лет: да или нет? ; PFAPA-syndrome (Marshall syndrome) in a 1.6-year-old child: yes or no?

Συγγραφείς: Korchagina, A. P., Lepeshkova, T. S., Корчагина, А. П., Лепешкова, Т. С.

Πηγή: Сборник статей

Θεματικοί όροι: MARSHALL SYNDROME, PFAPA SYNDROME, AUTO-INFLAMMATORY DISEASES, PERIODIC FEVER, PHARYNGITIS, СИНДРОМ МАРШАЛЛА, PFAPA-СИНДРОМ, АУТОВОСПАЛИТЕЛЬНЫЕ ЗАБОЛЕВАНИЯ, ПЕРИОДИЧЕСКАЯ ЛИХОРАДКА, ФАРИНГИТ

Περιγραφή αρχείου: application/pdf

Relation: Актуальные вопросы современной медицинской науки и здравоохранения: материалы VII Международной научно-практической конференции молодых учёных и студентов, Екатеринбург, 17-18 мая 2022 г.; http://elib.usma.ru/handle/usma/10010

Διαθεσιμότητα: http://elib.usma.ru/handle/usma/10010

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3

Academic Journal

The Clinical Course and Outcomes of Familial Mediterranean Fever in Crimean Tatar Patients: Preliminary Results of Case Series ; Течение и исходы семейной средиземноморской лихорадки у пациентов крымско-татарской национальности: предварительные результаты исследования серии случаев

Συγγραφείς: Olga V. Zhogova, Sergey V. Ivanovskiy, Natalya V. Lagunova, Anastasia V. Tumakova, Mikhail M. Kostik, О. В. Жогова, С. В. Ивановский, Н. В. Лагунова, А. В. Тумакова, М. М. Костик

Συνεισφορές: The article has been funded by Novartis. Company employees did not participate in planning, conducting and discussing of the results of this study., Статья опубликована при поддержке компании «Новартис». Сотрудники компании не участвовали в планировании, проведении и обсуждении результатов настоящего исследования.

Πηγή: Current Pediatrics; Том 19, № 3 (2020); 200-206 ; Вопросы современной педиатрии; Том 19, № 3 (2020); 200-206 ; 1682-5535 ; 1682-5527

Θεματικοί όροι: аутовоспалительные заболевания, familial Mediterranean fever, Crimean Tatar, periodic fever, autoinflammatory diseases, семейная средиземноморская лихорадка, крымские татары, периодическая лихорадка

Περιγραφή αρχείου: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

Relation: https://vsp.spr-journal.ru/jour/article/view/2396/941; https://vsp.spr-journal.ru/jour/article/view/2396/1000; Aksentijevich I, Kastner DL. Genetics of monogenic autoinflammatory diseases: past successes, future challenges. Nat Rev Rheumatol. 2011;7(8):469–478. doi:10.1038/nrrheum.2011.94.; Chae JJ, Wood G, Masters SL, et al. The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1beta production. Proc Natl Acad Sci U S A. 2006;103(26):9982–9987. doi:10.1073/pnas.0602081103.; Sohar E, Gafni J, Pras M, Heller H. Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med. 1967;43(2):227–253. doi:10.1016/0002-9343(67)90167-2.; Yilmaz E, Ozen S, Balci B, et al. Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. Eur J Hum Genet. 2001;9(7):553–555. doi:10.1038/sj.ejhg.5200674.; Touitou I. Standardized testing for mutations in familial Mediterranean fever. Clin Chem. 2003;49(11):1781–1782. doi:10.1373/clinchem.2003.025791.; Touitou I. The spectrum of Familial Mediterranean Fever (FMF) mutations. Eur J Hum Genet. 2001;9(7):473–483. doi:10.1038/sj.ejhg.5200658.; The International FMF Consortium. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell. 1997;90(4):797–807. doi:10.1016/s0092-8674(00)80539-5.; French FMFC. A candidate gene for familial Mediterranean fever. Nat Genet. 1997;17(1):25–31. doi:10.1038/ng0997-25.; Padeh S, Shinar Y, Pras E, et al. Clinical and diagnostic value of genetic testing in 216 Israeli children with Familial Mediterranean fever. J Rheumatol. 2003;30(1):185–190.; Marek-Yagel D, Berkun Y, Padeh S, et al. Clinical disease among patients heterozygous for familial Mediterranean fever. Arthritis Rheum. 2009;60(6):1862–1866. doi:10.1002/art.24570.; Booty MG, Chae JJ, Masters SL, et al. Familial Mediterranean fever with a single MEFV mutation: where is the second hit? Arthritis Rheum. 2009;60(6):1851–1861. doi:10.1002/art.24569.; Ece A, Cakmak E, Uluca U, et al. The MEFV mutations and their clinical correlations in children with familial Mediterranean fever in southeast Turkey. Rheumatol Int. 2014;34(2):207–212. doi:10.1007/s00296-013-2858-1.; Kastner DL, Aksentijevich I. Intermittent and periodic arthritis syndromes. In: Koopman WJ, Moreland LW, eds. Arthritis and allied conditions: a textbook of rheumatology. 15th ed. Philadelphia, USA: Lippincott Williams and Wilkins; 2005. pp. 1411–1461.; Жогова О.В., Лагунова Н.В., Ивановский С.В. и др. Семейная средиземноморская лихорадка в Республике Крым: описание серии случаев с анализом исторических и этнографических аспектов заболевания. Научно-практическая ревматология. — 2019. — Т. 57, № 3. — С. 339–344.; Tsuchiya-Suzuki A, Yazaki M, Nakamura A, et al. Clinical and genetic features of familial Mediterranean fever in Japan. J Rheumatol. 2009;36(8):1671–1676. doi:10.3899/jrheum.081278.; Lim AL, Jang HJ, Han JW, et al. Familial Mediterranean fever: the first adult case in Korea. J Korean Med Sci. 2012;27(11): 1424–1427. doi:10.3346/jkms.2012.27.11.1424.; Li J, Zhang Y, Wang W, et al. Three cases with familial Mediterranean fever misdiagnosed as juvenile idiopathic arthritis. Zhonghua Er Ke Za Zhi. 2017;55(5):383–387. doi:10.3760/cma.j.issn.0578-1310.2017.05.015.; Gattorno M, Hofer M, Federici S, et al. Classification criteria for autoinflammatory recurrent fevers. Ann Rheum Dis. 2019;78(8): 1025–1032. doi:10.1136/annrheumdis-2019-215048.; Ozen S, Demirkaya E, Erer B, et al. EULAR recommendations for the management of familial Mediterranean fever. Ann Rheum Dis. 2016;75(4):644–651. doi:10.1136/annrheumdis-2015-208690.; Livneh A, Langevitz P, Zemer D, et al. Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum. 1997;40(10): 1879–1885. doi:10.1002/art.1780401023.; Pras M. Familial Mediterranean fever: from the clinical syndrome to the cloning of the pyrin gene. Scand J Rheumatol. 1998;27(2): 92–97. doi:10.1080/030097498440949.; Yalcinkaya F, Cakar N, Misirlioglu M, et al. Genotypephenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis. Rheumatology (Oxford). 2000;39(1):67–72. doi:10.1093/rheumatology/39.1.67.; Ozen S, Demirkaya E, Amaryan G, et al. Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children. Ann Rheum Dis. 2014;73(4):662–667. doi:10.1136/annrheumdis-2012-202708.; Ozen S, Aktay N, Lainka E, et al. Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease. J Clin Rheumatol. 2013 Aug;19(5):246-51. doi:10.1097/RHU.0b013e31829ce005.; Berkun Y, Ben-Chetrit E, Klar A, Ben-Chetrit E. Peritoneal adhesions and intestinal obstructions in patients with familial Mediterranean fever are they more frequent? Semin Arthritis Rheum. 2007;36(5): 316–321. doi:10.1016/j.semarthrit.2006.11.002.; Barut K, Sahin S, Adrovic A, et al. Familial Mediterranean fever in childhood: a single-center experience. Rheumatol Int. 2018;38(1):67–74. doi:10.1007/s00296-017-3796-0.; Rawashdeh MO, Majeed HA. Familial Mediterranean fever in Arab children: the high prevalence and gene frequency. Eur J Pediatr. 1996;155(7):540–544. doi:10.1007/bf01957901.; Tunca M, Akar S, Onen F, et al. Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore). 2005;84(1):1–11. doi:10.1097/01.md.0000152370.84628.0c.; Mukhin NA, Kozlovskaya LV, Bogdanova MV, et al. Predictors of AA amyloidosis in familial Mediterranean fever. Rheumatol Int. 2015;35(7):1257–1261. doi:10.1007/s00296-014-3205-x.; Eshed I, Rosman Y, Livneh A, et al. Exertional leg pain in familial Mediterranean fever: a manifestation of an underlying enthesopathy and a marker of more severe disease. Arthritis Rheumatol. 2014;66(11):3221–3226. doi:10.1002/art.38797.; Jarjour RA, Al-Berrawi S. Familial Mediterranean fever in Syrian children: phenotype-genotype correlation. Rheumatol Int. 2015; 35(4):629–634. doi:10.1007/s00296-014-3116-x.; Manna R, Cerquaglia C, Curigliano V, et al. Clinical features of familial Mediterranean fever: an Italian overview. Eur Rev Med Pharmacol Sci. 2009;13 Suppl 1:51–53.; Colak S, Tekgoz E, Cinar M, Yilmaz S. The assessment of tocilizumab therapy on recurrent attacks of patients with familial Mediterranean fever: A retrospective study of 15 patients. Mod Rheumatol. 2020:1–3. doi:10.1080/14397595.2019.1709258.; Ugurlu S, Hacioglu A, Adibnia Y, et al. Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever. Orphanet J Rare Dis. 2017;12(1):105. doi:10.1186/s13023-017-0642-0.; Akar S, Cetin P, Kalyoncu U, et al. Nationwide experience with off-label use of interleukin-1 targeting treatment in Familial Mediterranean Fever patients. Arthritis Care Res (Hoboken). 2018; 70(7):1090–1094. doi:10.1002/acr.23446.; Gul A. Approach to the patients with inadequate response to colchicine in familial Mediterranean fever. Best Pract Res Clin Rheumatol. 2016 Apr;30(2):296-303. doi:10.1016/j.berh.2016.09.001.; De Benedetti F, Gattorno M, Anton J, et al. Canakinumab for the Treatment of Autoinflammatory Recurrent Fever Syndromes. N Engl J Med. 2018;378(20):1908–1919. doi:10.1056/NEJMoa1706314.; Laskari K, Boura P, Dalekos GN. Longterm Beneficial Effect of Canakinumab in Colchicine-resistant Familial Mediterranean Fever. J Rheumatol. 2017;44(1):102–109. doi:10.3899/jrheum.160518.

Διαθεσιμότητα: https://vsp.spr-journal.ru/jour/article/view/2396
https://doi.org/10.15690/vsp.v19i3.2115

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4

Academic Journal

Familial Mediterranean Fever: Current Approaches to Diagnosis and Treatment ; Семейная средиземноморская лихорадка: современные подходы к диагностике и лечению

Συγγραφείς: Mikhail M. Kostik, Olga V. Zhogova, Natalia V. Lagunova, Sergey V. Ivanovskiy, Oksana L. Kolobova, Larisa N. Melnikova, М. М. Костик, О. В. Жогова, Н. В. Лагунова, С. В. Ивановский, О. Л. Колобова, Л. Н. Мельникова

Συνεισφορές: Novartis, Компания «Новартис»

Πηγή: Current Pediatrics; Том 17, № 5 (2018); 371-380 ; Вопросы современной педиатрии; Том 17, № 5 (2018); 371-380 ; 1682-5535 ; 1682-5527

Θεματικοί όροι: канакинумаб, periodic fever, fever of unknown origin, interleukin 1, colchicine, anakinra, canakinumab, периодическая лихорадка, лихорадка неясного генеза, интерлейкин 1, колхицин, анакинра

Περιγραφή αρχείου: application/pdf

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https://doi.org/10.15690/vsp.v17i5.1953

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